Separation of 103Ru from a proton irradiated thorium matrix: A potential source of Auger therapy radionuclide103mRh

Tara Mastren, Valery Radchenko, Philip D. Hopkins, Jonathan W. Engle, John W. Weidner, Roy Copping, Mark Brugh, F. Meiring Nortier, Eva R. Birnbaum, Kevin D. John, Michael Ernst Heinrich Fassbender

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

Abstract

Ruthenium-103 is the parent isotope of 103mRh (t1/2 56.1 min), an isotope of interest for Auger electron therapy. During the proton irradiation of thorium targets, large amounts of 103Ru are generated through proton induced fission. The development of a two part chemical separation process to isolate 103Ru in high yield and purity from a proton irradiated thorium matrix on an analytical scale is described herein. The first part employed an anion exchange column to remove cationic actinide/lanthanide impurities along with the majority of the transition metal fission products. Secondly, an extraction chromatographic column utilizing diglycolamide functional groups was used to decontaminate 103Ru from the remaining impurities. This method resulted in a final radiochemical yield of 83 ± 5% of 103Ru with a purity of 99.9%. Additionally, measured nuclear reaction cross sections for the formation of 103Ru and 106Ru via the 232Th(p,f)103,106Ru reactions are reported within.

Original languageEnglish
JournalPLoS ONE
Volume12
Issue number12
DOIs
StatePublished - Dec 2017

Funding

We gratefully recognize the United States Department of Energy, Office of Science, Isotope Development and Production for Research and Application subprogram within Office of Nuclear Physics and the LANL LDRD program (LDRD 20160439ER) for financial support.

FundersFunder number
U.S. Department of Labor
Nuclear Physics
Laboratory Directed Research and Development20160439ER

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